BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to an oxygen-deficient perovskite type oxide superconductor,
more particularly to the improvement of the oxide superconductor comprising at least
one of yttrium and rare earth metals, at least one of alkaline earth metals, and copper
and oxygen. In other words, the present invention relates to the improvement of the
oxide superconductor represented by A₁B₂C₃D
7-δ, wherein A is at least one of yttrium and rare earth metals, B at least one of alkaline
earth metals, C copper and D oxygen.
Related Art
[0002] The oxygen-deficient perovskite type oxide sperconductors are known to have a superconducting
critical temperature Tc in oders of 90 K. Furthermore, some superconductors comprised
mainly of yttrium, barium, copper and oxygen and modified by partial substitution
for each component are known. For example,
Physical Review Letters, Vol. 58, No. 24, 1987, pp. 2579-2581, discusses that a superconductor comprising
yttrium, barium, copper, oxygen and fluorine may have a Tc of 100 K or higher.
Physical Review B, Vol. 36, No. 4, 1987, pp. 2308-2310, refers to a superconductor of yttrium- barium-copper
oxide wherein aluminum is partially substituted for the yttrium, represented by (Y
1-xAl
x) Ba₂Cu₃O
y.
Japanese Journal of Applied Physics, Vol. 26, No. 8, August 1987, pp. L1356-L1358, shows a superconductor having the
formula of (Y
1-xSc
x) (Ba
1-xSr
x) Cu₃O
y.
Journal of the American Chemical Society, 1987, 109, pp. 2848-2849, discloses a superconductor having a formula of RBa₂Cu₃O
y wherein R is Y, Nd, Sm, Eu, Gd, Dy, Ho, Yb, Lu or Sc. In Abstracts No. 3 of the lecture
in the Submeeting of the Japanese Physical Society, Autumn 1987, A. Yamasaki et al
teach use of Bi and discuss the superconductivity of a Bi-Sr-Cu-O system. Furthermore,
in
Japanese Journal of Applied Physics, Vol. 26, No. 12, December, 1987, pp. L2080-L2081, J. Akimitsu et al discuss the
superconductivity in the Bi-Sr-Cu-O system.
[0003] Particularly,
Physical Review Letters, Vol. 58, No. 24, pp. 2579-2581 above reports that a superconductor having a critical
temperature Tc of 155 K was obtained by substituting fluorine for part of oxygen.
[0004] On the other hand, it is known that the superconducting property of an yttrium-barium-copper-oxygen
system superconductor is greatly changeable depending upon a degree of oxygen deficiency.
Thus, the degree of oxygen deficiency is in general controlled by heat treating the
superconductors.
[0005] However, in the prior art it is also known to be very difficult to control a degree
of oxygen deficiency, degree of fluorine deficiency and proportion of oxygen atoms
and fluorine atoms. In the case that an amount of fluorine is substituted for part
of oxygen, the superconducting property varies depending upon the controlled degrees
of oxygen deficiency and fluorine deficiency, the proportions of oxygen atoms and
fluorine atoms and the positions of the substituted atoms.
[0006] The superconducting property gets unstable when fluorine atoms are substituted for
oxygen atoms at the positions of the oxygen atoms, because the property relies principally
on the electronic or magnetic properties of the binary structure of Cu-O atoms. Thus,
the property changes with time.
[0007] In order to increase the critical temperature Tc without any such change with time,
the electronic or magnetic properties of the Cu-O structure is necessary to be changed
by partially substituting for Y or Ba at its position another element.
SUMMARY OF THE INVENTION
[0008] The object of the present invention is to provide an oxygen-deficient type perovskite
oxide superconductor having an A-B-C-D structure wherein A is at least one of yttrium
and rare earth metals, B at least one of alkaline earth metals, C copper and D oxygen,
and having a critical temperature of higher than that of YBa₂Cu₃O
7-δ, i.e., having a critical temperature of about 100 or higher, given by substituting
for part of A at least one of the elements of Atomic Numbers 81 to 83.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] Fig. 1 is a graph showing a relationship between the superconducting critical temperature
of a Y-Ba-Cu-O system oxide superconductor and the amount of Bi or Tl substituted
for part of Y.
[0010] Fig. 2 is a graph showing a relationship between the temperature and resistivity
of a Y-Ba-Cu-O system oxide superconductor in which Bi is substituted for part of
Y.
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
[0011] In accordance with the present invention, there is provided an oxygen-deficient type
oxide superconductor having an A-B-C-D structure wherein A is at least one of yttrium
and rare earth metals, B at least one of alkaline earth metals, C copper and D oxygen,
in which at least one of elements of Atomic Numbers 81 to 83 are substituted for part
of A.
[0012] As the alkaline earth metals may be used any of barium, strontium, calcium and magnesium.
[0013] The Atomic Numbers 81 to 83 are thallium (Tl), lead (Pb) and bismuth (Bi), respectively.
[0014] As the rare earth metals may be used at least one of lanthanum (La), cerium (Ce),
praseodymium (Pr), neodymium (Nd), samarium (Sm), europium (Eu), gadolinium (Gd),
terbium (Tb), dysprosium (Dy), holmium (Ho), erbium (Er), thulium (Tm), ytterbium
(Yb) and lutetium (Lu).
[0015] When the elements to be substituted for part of A are referred to as E, i.e., the
superconductor is represented by A
1-xE
xBCD, the substituted amount x of E is desirably 0.05 to 0.95 for thallium, 0.05 to
0.5 for lead and 0.05 to 0.6 for bismuth.
[0016] Preferred combinations of components of the oxide superconductor according to the
present invention are Y-Tl-Ba-Ca-Cu-O, Y-Bi-Ba-Cu-O, Y-Bi-Sr-Ca-Cu-O and Y-Tl-Ba-Cu-O.
[0017] When Tl is substituted for part of A, the oxide superconductor having a superconducting
critical temperature Tc of 110 K or higher may be obtained.
[0018] When Bi is substituted for part of A, the oxide superconductor having a superconducting
critical temperature Tc of 90 K or higher may be obtained.
[0019] When Pb is substituted for part of A, the oxide superconductor having a superconducting
critical temperature Tc of 100 K or higher may be obtained.
[0020] The present invention particularly provides an oxygen-deficient type oxide superconductor
having a formula of A₁B₂C₃D
7-δ wherein A is at least one of yttrium and rare earth metals, B at least one of alkaline
earth metals, C copper and D oxygen, featured by substituting at least one of elements
of Atomic Numbers 81 to 83 for part of A.
[0021] The amount of δ in the superconductor oxide A₁B₂C₃D
7-δ represents a degree of oxygen deficiency (0 ≦ δ ≦ 1). When δ is in the range of less
than 0.3, the sperconductor oxide is in an orthorhombic form and, when δ is more than
0.3, it is in a tetragonal form.
[0022] From many experiments regarding quantization of magnetic flux or alternating-current
Josephson effect, it has been confirmed until now that with oxide superconductors
having a superconducting critical temperature of 90 K or higher, a carrier for superconductive
current has an electric charge of 2e. Thus, it is known that the carrier is a pair
of electric charge 2e (Cooper pair), but it has not yet been clarified which of lattice
vibration (phonon), fluctuation of electric charge (exciton and etc.) or magnetic
fluctuation has an effect on superconductivity.
[0023] However, from various experiments on oxide superconductors of 90 K or higher, it
is considered that the pair of electrons is made due to the strong direct correlation
of the electrons with each other (magnetic fluctuation). The strong direct correlation
of electrons with each other is considered to mean that the pair of superconducting
electrons is made due to the mutual action of spins possessed by the electrons. In
other words, interaction between the electrons of each copper atom in the Cu-O-Cu
bond (interaction between the spins of the electrons) is significant to the mechanism
of giving the superconducting properties. This interaction is intensified by substituting
Bi, Tl and/or Pb for part of A of the A-B-C-D superconductor, to achieve a higher
critical temperature Tc.
[0024] In accordance with the present invention, it has been found that a superconducting
critical temperature Tc of 100 K or higher is achieved by substituting Bi, Tl or Pb
for part of A of the A-B-C-D superconductor having a critical temperature in the orders
of 90 K. This is contributed to by a long mean free path of Bi, Tl and Pb which strengthens
the mutual action of electrons in Cu-O-Cu bonds.
[0025] According to the present invention, there are given such advantages that the superconducting
critical temperature Tc of an oxide superconductor represented by A-B-C-D werein A
is at least one of yttrium and rare earth metals, B at least one of alkaline earth
metals, C copper and D oxygen, can be raised up to 100 K or higher by substituting
Bi, Tl or Pb for part of A, further Tc is not changed with time, and the stable superconductivity
can be obtained at a temperature exceeding that of liquid nitrogen.
[0026] Furthermore, since the superconducting critical temperature of the oxide superconductor
according to the present invention is much higher than the cooling medium temperature
(77 K for liquid nitrogen), this oxide superconductor can be used as, for example,
various electronics devices or apparatuses for energy with a broader operation margin.
Therefore, the scope of applications of the oxide superconductors can be broadened.
[0027] The present invention will be further illustrated below with reference to some examples.
EXAMPLE 1
[0028] Fig. 1 is a graph showing a relationship between the amount (x) of Bi substituted
for part of Y in a Y-Ba-Cu-O oxide superconductor and the superconducting critical
temperature Tc of the oxide superconductor.
[0029] This oxide superconductor was made by a sputtering method. A spputering target used
was comprised of a BaCuO₂ target of 100 mm in diameter and 5 mm thick having Y and
Cu chips of 5 mm x 5 mm x 1 mm thick placed thereon. Sputtering was carried out so
that the composition of a film made was in a Y:Ba:Cu ratio of 1:2:3. Then, a Bi chip
or Tl chip was substituted for part of the Y chip, so that the amount (x) of Bi or
Tl in the resultant film was in the range of 0 to 1. Sputtering conditions are shown
in Table 1.

[0030] A thin film of about 1 µm thick was prepared under the sputtering conditions as shown
in Table 1. After the sputtering, the thin film was subjected to heat treatment in
an oxygen atmosphere at 900 to 1000°C for 2 hours. The heat treatment was carried
out at a cooling rate of 1°C/min.
[0031] As shown in Fig. 1, Tc is 100 K or higher when an amount x of Bi substituted is in
the range of 0.05 ≦ x ≦ 0.5. When an amount x of Bi substituted is higher than 0.6,
Tc is 90 or higher. Furthermore, Tc is 110 K or higher at an amount of Tl substituted
in the range of 0.15 ≦ x ≦ 0.5, and Tc is 90 K or higher at an amount of Tl in the
range of 0.05 ≦ x ≦ 0.95.
[0032] The value of Tc was measured herein by a usual four-probe method.
[0033] Fig. 2 is a temperature-resistivity graph shown at the Bi amount x of 0.3. The X-ray
diffraction pattern revealed that the thin film was in an orthorhombic form at the
Bi amount x of 0.3, and it had diffraction peaks which appear to indicate crystals
in a form other than the orthorhombic form at the Bi amount x of greater than 0.6.
In the latter case, such crystals had a Tc of 90 K or lower. When the Bi amount x
substituted was 1, i.e., Y was entirely replaced with Bi, no superconductivity was
observed.
[0034] Thus, it was found that the oxide superconductors of (Y
1-xBi
x)₁Ba₂Cu₃O
7-δ or (Y
1-xTl
x)₁Ba₂Cu₃O
7-δ had a high critical temperature at the Bi amount x substituted of 0.05 to 0.6, and
at the Tl amount x substituted 0.05 to 0.95. Furthermore, the obtained thin film having
a Tc ≧ 100 K had no change observed in its properties even when it was left to stand
for a long period of time.
EXAMPLE 2
[0035]
(*) z denotes the amount of oxygen and varies depending upon proportions of a, b and
c and various conditions for preparing the oxide.
(**) d is oxygen which is present in an amount (z) not determinable according to the
state of the art and which fact is known to the art
[0036] This example concerns an oxide superconductor of a Y-Bi-Sr-Ca-Cu-O system.
[0037] As starting materials were used Y₂O₃, Bi(NO₃), SrCO₃ CaCO₃ and CuO. These materials
were mixed so that the obtained compositions were Y₁Bi₁Sr₁Ca₁Cu₂O
z(*) (A₂B₂C₂D
z) and Y
0·1Bi
0·9Sr₁Ca₁Cu₂O
z (A₁B₂C₂D
z) (**), respectively. Both were fired at a temperature of 870°C.
[0038] The superconducting critical temperature Tc of Y₁Bi₁Sr₁Ca₁Cu₂O
z was 120 K and that of Y
0·1Bi
0·9Sr₁Ca₁Cu₂O
z was 110 K.
EXAMPLE 3
[0039] This example concerns the oxides of Y-Tl-Ba-Cu-O and Y-Tl-Ba-Ca-Cu-O systems.
[0040] As starting materials were used Y₂O₃, Tl₂O₃, BaCO₃, CaCO₃ and CuO. These materials
were mixed so that the desired compositions were obtained, and fired.
[0041] Table 2 shows that the compositions of the obtained oxide superconductors, firing
temperatures and superconducting critical temperatures Tc. Furthermore, Table 2 shows
an oxide of a Y-Ba-Cu-O system.

[0042] The superconducting critical temperature could be raised by substituting Tl for part
of Y.
EXAMPLE 4
[0043] This example concerns the oxide superconductor of a Y-Pb-Sr-Ca-Cu-O system.
[0044] As the starting materials were used Y₂O₃, Pb(NO₃), SrCO₃, CaCO₃ and CuO. These materials
were mixed so that the composition of Y
0·5Pb
0·5Sr₁Ca₁Cu₃O
7-δ was obtained, and fired at 870°C.
[0045] The superconducting critical temperature Tc was 120 K.
1. An oxygen-deficient perovskite type oxide superconductor represented by the formula
of A-B-C-D, wherein A is at least one of yttrium and rare earth metals of Atomic Numbers
57 to 71, except for Atomic Number 61, B is at least one of alkaline earth metals,
C is copper and D is oxygen, said oxide superconductor containing at least one of
elements of Atomic Numbers 81 to 83 substituted for part of A.
2. The oxide superconductor according to Claim 1, wherein A denotes Y1-xTlx wherein an amount x of Tl substituted is equal to or greater than 0.05 but equal
to or smaller than 0.95.
3. The oxide superconductor according to Claim 2, wherein said oxide has a superconducting
critical temperature of 110 K or higher.
4. The oxide superconductor according to Claim 1, wherein A denotes Y1-xBix wherein an amount x of Bi substituted is equal to or greater than 0.05 but equal
to or smaller than 0.6.
5. The oxide superconductor according to Claim 4, wherein said oxide has a superconducting
critical temperature of 90 K or higher.
6. The oxide superconductor according to Claim 1, wherein A denotes Y1-xPbx wherein an amount x of Pb substituted is equal to or greater than 0.05 but equal
to or smaller than 0.5.
7. The oxide superconductor according to Claim 6, wherein said oxide has a superconducting
critical temperature of 100 K or higher.
8. The oxide superconductor according to Claim 1, wherein said alkaline earth metal
is at least one selected from barium, calcium, strontium and magnesium.
9. The oxide superconductor according to Claim 1, wherin said oxide is of a Y-Tl-Ba-Ca-Cu-O,
Y-Bi-Ba-Cu-O, Y-Bi-Sr-Ca-Cu-O, or Y-Tl-Ba-Cu-O system.
10. An oxyten-deficient perovskite type oxide superconductor represented by one of
the formulae of A₁B₂C₃D7-δ, A₂B₂C₂Dz and A₁B₂C₂Dz, wherein A is at least one of yttrium and rare earth metals of Atomic Numbers 57
to 71, except for Atomic Number 61, B is at least one of alkaline earth metals, C
is copper and D is oxygen, said oxide superconductor containing at least one of elements
of Atomic Numbers 81 to 83 substituted for part of A.
11. The oxide superconductor according to Claim 10, wherein A denotes Y1-xTlx wherein an amount x of Tl substituted is equal to or greater than 0.05 but equal
to or smaller than 0.95.
12. The oxide superconductor according to Claim 11, wherein said oxide has a superconducting
critical temperature of 110 K or higher.
13. The oxide superconductor according to Claim 10, wherein A denotes Y1-xBix wherein an amount x of Bi substituted is equal to or greater than 0.05 but equal
to or smaller than 0.6.
14. The oxide superconductor according to Claim 13, wherein said oxide has a superconducting
critical temperature of 90 K or higher.
15. The oxide superconductor according to Claim 10, wherein A denotes Y1-xPbx wherein an amount x of Pb substituted is equal to or greater than 0.05 but equal
to or smaller than 0.5.
16. The oxide superconductor according to Claim 15, wherein said oxide has a superconducting
critical temperature of 100 K or higher.
17. The oxide superconductor according to Claim 10, wherein said alkaline earth metal
is at least one selected from barium, calcium, strontium and magnesium.
18. The oxide superconductor according to Claim 10, wherein said oxide is of a Y-Tl-Ba-Ca-Cu-O,
Y-Bi-Ba-Cu-O, Y-Bi-Sr-Ca-Cu-O, or Y-Tl-Ba-Cu-0 system.
19. The oxide superconductor according to Claim 10, said oxide having a formula of
Y0·2Tl0·8Ba₁Ca₁Cu₂Oz and a superconducting critical temperature of 128 K.
20. The oxide superconductor according to Claim 10, said oxide having a formula of
Y₁Bi₁Sr₁Ca₁Cu₂Oz and a superconducting critical temperature of 120 K.
21. The oxide superconductor according to Claim 10, said oxide having a formula of
Y0·1Bi0·9Sr₁Ca₁Cu₂Oz and a superconducting critical temperature of 110 K.